Catheter kit

ABSTRACT

A catheter kit includes a catheter having an optical fiber, and a catheter accommodating tool which accommodates the catheter. The catheter accommodating tool has a tubular hoop, and a position adjustment mechanism provided at the hoop. The hoop has a hoop tip end portion at which a catheter tip end portion, from which laser light transmitted through the optical fiber is emitted, is disposed, and a hoop base end portion which is opposite to the hoop tip end portion. The position adjustment mechanism is provided at the hoop base end portion and changes a position of the catheter tip end portion with respect to the hoop tip end portion.

TECHNICAL FIELD

The present invention relates to a catheter kit which accommodates acatheter with a built-in optical fiber.

BACKGROUND ART

A catheter with a built-in optical fiber is used for patient diagnosisand treatment. For example, Patent Document 1 discloses this inthrombolytic therapy. When a catheter is used for thrombolytic therapy,the catheter is first inserted into a patient's body. Thereafter, anaffected area is irradiated with laser light through the catheter.

CITATION LIST Patent Literature

[Patent Literature 1] Japanese Patent No. 4409499

[Patent Literature 2] Japanese Examined Utility Model Publication No.H6-42182

[Patent Literature 3] Japanese Unexamined Patent Publication No.H8-262278

SUMMARY OF INVENTION Technical Problem

The catheter is inserted into a body at the time of use. Therefore, whenthe catheter is inserted into the body, it is required to besufficiently sterilized. Therefore, during storage and transportation,the catheter is accommodated in a tubular container called a hoop tomaintain cleanliness. Thus, in order to maintain the cleanliness of thecatheter, it is desirable to store the catheter in the hoop untilimmediately before use.

In a method disclosed in Patent Document 1, it is desirable to irradiatean affected area with laser light having a predetermined intensity.Therefore, as disclosed in Patent Documents 2 and 3, a light intensityconfirmation operation is performed immediately before start of atreatment.

Therefore, an object of the present invention is to provide a catheterkit allowing a light intensity confirmation operation to be performedeasily while maintaining cleanliness of a catheter.

Solution to Problem

A catheter kit according to one aspect of the present invention includesa catheter having an optical fiber, and a catheter accommodating toolwhich accommodates the catheter, wherein the catheter accommodating toolincludes a tubular hoop, and a position adjustment mechanism provided atthe hoop, the hoop has a hoop tip end portion at which a catheter tipend portion from which light transmitted through the optical fiber isemitted is disposed, and a hoop base end portion which is opposite tothe hoop tip end portion, and the position adjustment mechanism changesa position of the catheter tip end portion with respect to the hoop tipend portion.

According to such a catheter kit, it is possible to measure lightintensity in a state in which the catheter is accommodated in the hoop.Therefore, cleanliness of the catheter can be maintained, and a lightintensity confirmation operation can be easily performed. Furthermore,according to such a catheter kit, it is possible to mutually change theposition of the catheter tip end portion at the time of storage and theposition of the catheter tip end portion at the time of measurement.That is, at the time of storage, it is possible to dispose the cathetertip end portion on the inner side of the hoop tip end portion. As aresult, the catheter tip end portion can be protected. Furthermore, atthe time of measurement, it is possible to align the catheter tip endportion with the hoop tip end portion. As a result, it is possible tocurb occurrence of variation in a distance from the catheter tip endportion to a light receiving part.

The catheter accommodating tool may further include a closing partprovided at an end portion of the hoop, and the closing part may have atransmission window which transmits the light emitted from the catheter.According to such a configuration, it is possible to reliably protectthe catheter tip end portion and to measure the light intensity.

The end portion of the hoop may have an opening, the catheter tip endportion from which the light transmitted through the optical fiber isemitted may be disposed at the end portion of the hoop, and thetransmission window may close the opening and transmits the light. Thisconfiguration also reliably protects the catheter tip end portion andallows measurement of the light intensity.

The closing part may be a cap member which is detachably mounted to thehoop. According to such a configuration, the configuration of the hoopend portion can be selected according to the form of measurement of thelight intensity. That is, it is possible to select a mode in which themeasurement is performed while the end portion from which light isemitted is protected, and a mode in which measurement is performed whilelight is directly incident on a measurement device.

The closing part may be a cover part which is a part of the hoop and isintegrated with the hoop. According to such a configuration, the coverpart is not separated from the hoop. As a result, the tip end portion ofthe catheter is reliably protected.

The hoop may have a through hole which extends in a directionintersecting a longitudinal direction of the hoop and extends from anouter circumferential surface to an inner circumferential surface.According to such a configuration, a sterilization gas can beappropriately provided to the catheter accommodated in the hoop.

Advantageous Effects of Invention

According to the present invention, a catheter kit capable ofmaintaining cleanliness of a catheter and easily performing a lightintensity confirmation operation is provided.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a view showing a configuration of a light measurement deviceaccording to an embodiment.

FIG. 2 is an enlarged cross-sectional view showing a configuration of anadapter and a catheter kit shown in FIG. 1 .

FIG. 3 is a cross-sectional view for explaining an operation of aposition adjustment mechanism.

FIG. 4 is a flowchart showing a main process of a light measurementmethod according to the first embodiment.

FIG. 5 is a view for explaining the main process shown in FIG. 4.

FIG. 6 is a view for explaining a main process following the processshown in FIG. 5 .

FIG. 7 is a view for explaining a main process following the processshown in FIG. 6 .

FIG. 8 is a perspective view showing a cross section of a catheter kitaccording to first, second and third modified examples.

FIG. 9 is a side view showing a cross section of a catheter kitaccording to fourth, fifth and sixth modified examples.

FIG. 10 is a side view showing a cross section of a catheter kitaccording to a seventh modified example.

FIG. 11 is a plan view showing a catheter kit according to an eighthmodified example.

FIG. 12 is a side view showing a cross section of a catheter kitaccording to ninth, tenth and eleventh modified examples.

FIG. 13 is a perspective view showing a cross section of a catheter kitaccording to twelfth and thirteenth modified example.

DESCRIPTION OF EMBODIMENTS

Hereinafter, embodiments of the present invention will be described indetail with reference to the attached drawings. In the description ofthe drawings, the same elements will be designated by the same referencesymbols, and duplicate descriptions will be omitted.

As shown in FIG. 1 , a light measurement device 1 measures an intensityof laser light L. The laser light L is provided from a light source 101to a catheter kit 30. Then, the laser light L is emitted from thecatheter kit 30. The light measurement device 1 includes a power meter 2and an adapter 3 (a second adapter). In the following description, theside of the respective elements from which light is emitted is referredto as a “tip end.” The side opposite to the “tip end” is referred to asa “base end.” For example, in the catheter kit 30, an end portion whichemits the laser light L is a “tip end portion.” An end portion whichreceives the laser light L is a “base end portion.”

The power meter 2 includes a case body 4, a light receiving part 6, amounting part 7, and a processing device 8.

The case body 4 holds a relative positional relationship between thelight receiving part 6 and the mounting part 7. The case body 4 isformed of an opaque material. The case body 4 and the adapter 3constitute a closed space. The light receiving part 6 is disposed insidethe closed space. According to such a configuration, it is possible toprevent stray light from being incident on the light receiving part 6.

The light receiving part 6 receives the laser light L output from thecatheter kit 30. The light receiving part 6 includes, for example, alight absorber. The light receiving part 6 converts absorbed light intoheat. Thereafter, the light receiving part 6 outputs a change of heat asa change in an electrical signal. For example, the light absorber mayinclude 3A-P manufactured by Ophir, and the like. The electrical signaloutput from the light receiving part 6 is transmitted to the processingdevice 8 via a signal cable. The processing device 8 obtains theintensity of the light received by the light receiving part 6 on thebasis of the electrical signal. Then, the processing device 8 displaysan intensity value thereof.

The mounting part 7 is provided at a position facing the light receivingpart 6. The mounting part 7 may be part of the case body 4. The mountingpart 7 defines a position of the catheter kit 30 with respect to thelight receiving part 6. The position of the catheter kit 30 with respectto the light receiving part 6 includes a distance from a tip end portionof the catheter kit 30 to the light receiving part 6 in a travelingdirection of the laser light L emitted from the catheter kit 30.Furthermore, the position includes a position of the tip end portion ofthe catheter kit 30 with respect to the light receiving part 6 in aplane orthogonal to the traveling direction of the laser light L. Themounting part 7 has a standing tubular part 7 a which protrudes from thecase body 4. Furthermore, the standing tubular part 7 a has an adapterarrangement part 7H which is a through hole. The catheter kit 30 isdisposed in the adapter arrangement part 7H via the adapter 3. A tip endof the adapter arrangement part 7H is a tip end opening 7Ha provided inan inner wall of the case body 4. A base end of the adapter arrangementpart 7H is a base end opening 7Hb provided in an end portion of themounting part 7.

As shown in FIG. 2 , the adapter 3 allows the catheter kit 30 to bemounted in the power meter 2. The adapter 3 may be formed of, forexample, polyacetal. The adapter 3 has an adapter main body 9 and anadapter flange 11. The adapter main body 9 and the adapter flange 11 areintegrally formed. The adapter main body 9 is disposed in the adapterarrangement part 7H. The adapter main body 9 has an adapter tip endsurface 3 a. A male thread may be provided on an outer circumferentialsurface of the adapter main body 9. The adapter flange 11 is provided onthe base end side. The adapter flange 11 has an adapter base end surface3 b. An outer diameter of the adapter flange 11 is larger than an innerdiameter of the adapter arrangement part 7H. The adapter flange 11 maybe in contact with a mounting end surface 7 b of the mounting part 7.

The adapter 3 has a hoop arrangement part 3H which holds a tip end ofthe catheter kit 30. The hoop arrangement part 3H is a hole whichextends from the adapter base end surface 3 b toward the adapter tip endsurface 3 a. Also, the base end side of the hoop arrangement part 3H isa base end opening 3Hb provided in the adapter base end surface 3 b. Thebase end opening 3Hb may be chamfered (tapered). An adapter tip end wall3 d is provided on the tip end side of the hoop arrangement part 3H.When the catheter kit 30 is disposed in the hoop arrangement part 3H,the tip end of the catheter kit 30 is in contact with the adapter tipend wall 3 d. More specifically, a tip end surface of a protection cap43 which will be described later is in contact with the adapter tip endwall 3 d. Thus, the adapter tip end wall 3 d defines an insertion depthof the catheter kit 30 with respect to the adapter 3. A light passingpart 3 e which is a through hole is provided in the adapter tip end wall3 d. The light passing part 3 e guides the laser light L emitted fromthe catheter kit 30 to the light receiving part 6. Therefore, a contactpart 3 c (a second contact part) is constituted by the adapter tip endwall 3 d and the light passing part 3 e.

Next, the catheter kit 30 will be described in detail. The catheter kit30 includes a catheter 31 and a catheter accommodating tool 32. Thecatheter 31 has a built-in optical fiber 33. The catheter 31 may alsoinclude other components 34 required for treatment and examination, inaddition to the optical fiber 33. The optical fiber 33 has an opticalfiber tip end portion 33 a and an optical fiber base end portion 33 b.The optical fiber tip end portion 33 a is inserted into a human body.Furthermore, the optical fiber tip end portion 33 a emits the laserlight L. The light source 101 (refer to FIG. 1 ) is connected to theoptical fiber base end portion 33 b. Additionally, the laser light L isprovided to the optical fiber base end portion 33 b.

The catheter accommodating tool 32 accommodates the catheter 31. Thecatheter accommodating tool 32 includes a hoop 36, a holding plug 37 (acatheter holding part), the protection cap 43, and a bellows 46 (referto FIG. 1 ).

The hoop 36 has a tubular pipe shape. The hoop 36 described in theembodiment is used at a medical site. The hoop 36 refers to a resin tubeinto which the catheter 31 is inserted. The hoop 36 does not have to beflexible. The hoop 36 may be flexible or non-flexible. The hoop 36includes a hoop tip end portion 36 a in which a catheter tip end portion31 a is disposed, and a hoop base end portion 36 b in which the catheterbase end portion 31 b side is disposed. A tip end opening 36 c isprovided in the hoop tip end portion 36 a. That is, the hoop tip endportion 36 a is not closed. In other words, the hoop tip end portion 36a is open. The hoop base end portion 36 b also has a base end opening 36d. That is, the hoop base end portion 36 b is also not closed. In otherwords, the hoop base end portion 36 b is open. A gas introduction hole36 e is provided in the hoop 36. The gas introduction hole 36 e isprovided in a side wall of the hoop 36. Additionally, the gasintroduction hole 36 e passes therethrough from an outer circumferentialsurface to an inner circumferential surface.

Here, a relationship between an inner diameter (f) and an outer diameter(d) of the hoop 36 and an inner diameter (e) of the light passing part 3e of the adapter 3 is f<e<d. According to this dimensional relationship,it is possible to prevent the catheter tip end portion 31 a from cominginto contact with an unsterilized portion.

The holding plug 37 is disposed to be press-fitted into the base endopening 36 d on the side of the hoop base end portion 36 b. The holdingplug 37 includes a catheter arrangement part 38, a press-fit part 39which is press-fitted into the hoop 36, and a flange part 41. Thecatheter arrangement part 38 is a through hole which holds the catheter31. The holding plug 37 holds the position of the catheter 31 withrespect to the hoop 36 when inserted into the hoop 36. That is, theholding plug 37 is fixed to the hoop 36. Additionally, the holding plug37 holds the catheter 31. Thus, the holding plug 37 inserted into thehoop 36 holds the position of the catheter 31 with respect to the hoop36.

The catheter arrangement part 38 is disposed on the side of the catheterbase end portion 31 b. An inner diameter of the catheter arrangementpart 38 is slightly smaller than an outer diameter of the catheter 31.According to such a configuration, an inner circumferential surface ofthe catheter arrangement part 38 is press-fitted onto an outercircumferential surface of the catheter 31. As a result, the position ofthe catheter 31 with respect to the holding plug 37 is held. Thepress-fit part 39 is press-fitted into the hoop 36 from the base endopening 36 d of the hoop base end portion 36 b. An outer diameter of thepress-fit part 39 is slightly larger than an inner diameter of the hoop36. According to such a configuration, an outer circumferential surfaceof the press-fit part 39 is press-fitted into an inner circumferentialsurface of the hoop 36. As a result, a position of the holding plug 37with respect to the hoop 36 is held. The flange part 41 is provided onthe base end side of the press-fit part 39. An outer diameter of theflange part 41 is larger than an inner diameter of the hoop 36.

The protection cap 43 is mounted on the hoop 36. The protection cap 43has a tubular shape of which one end is closed and the other end isopen. The protection cap 43 may be formed of, for example, acrylic. Theprotection cap 43 closes the tip end opening 36 c of the hoop tip endportion 36 a. According to such a configuration, the catheter tip endportion 31 a is protected. Further, the protection cap 43 transmits thelaser light L emitted from the catheter tip end portion 31 a. Theprotection cap 43 has a cap tip end portion 43 a and a cap base endportion 43 b. The cap tip end portion 43 a has a transmission window 43c. The transmission window 43 c closes the tip end opening 36 c.Furthermore, the transmission window 43 c transmits the laser light L.The cap base end portion 43 b has a base end opening 43Hb of the hooparrangement part 43H into which the hoop 36 can be inserted.

The bellows 46 is disposed between the hoop 36 and the holding plug 37.The bellows 46 which is a so-called bellows tube can extend and contractin an axial direction thereof. The bellows 46 has an elasticity tomaintain a predetermined length when no external force is applied. Forexample, when the bellows 46 is pressed in the axial direction, a lengthof the bellows 46 is reduced. On the other hand, when the pressing isstopped, the length of the bellows 46 returns to the length before thepressing.

The bellows 46 has a bellows tip end portion 46 a and a bellows base endportion 46 b. The bellows tip end portion 46 a is in contact with thehoop base end portion 36 b. The bellows base end portion 46 b is incontact with the flange part 41 of the holding plug 37. According tosuch a configuration, a constant gap is maintained between a base endsurface of the hoop base end portion 36 b and an end surface of theflange part 41 of the holding plug 37 (refer to a gap D1 in FIG. 3(a)).On the other hand, it is assumed that the holding plug 37 is pushed tothe hoop 36 side and the press-fit part 39 of the holding plug 37 ispressed into the hoop 36. Also in this case, a restoring force of thebellows 46 is generated. However, the restoring force is smaller than africtional force between the press-fit part 39 and the innercircumferential surface of the hoop 36. Accordingly, a state in whichthe holding plug 37 is pushed to the hoop 36 side is maintained (referto a gap D2 in FIG. 3(b)). The bellows 46 may not generate the restoringforce. In this case, the bellows 46 can maintain a stretched state (thatis, a state of FIG. 3(a)) and a contracted state (a state of FIG. 3(b))without requiring additional components.

That is, with the bellows 46 and the holding plug 37, the position ofthe catheter 31 with respect to the hoop 36 can be switched to a firstposition or a second position. Therefore, the bellows 46 and the holdingplug 37 constitute a position adjustment mechanism 47 (a positionadjusting part). First, when the holding plug 37 is in a state in whichit is not pushed into the hoop 36, the catheter 31 is held at the firstposition. In the first position, the catheter tip end portion 31 a isdisposed closer to the base end from the hoop tip end portion 36 a(refer to FIG. 3(a)). Here, a gap from a tip end surface of the hoop tipend portion 36 a to a tip end surface of the catheter tip end portion 31a is D3. The gap D3 is obtained by subtracting the gap D2 from the gapD1 (D3=D1−D2). On the other hand, when the holding plug 37 is in a statein which it is pushed into the hoop 36, the catheter 31 is held at thesecond position. In this second position, the positions of the hoop tipend portion 36 a and the catheter tip end portion 31 a coincide witheach other (refer to FIG. 3(b)).

Next, a light intensity measurement method using the light measurementdevice 1 will be described with reference to a flowchart shown in FIG. 4. First, a process of preparing the catheter kit 30 will be described.

Step S2 is carried out (refer to FIG. 5(a)). First, the protection cap43 is mounted on the hoop 36. In Step S2, the protection cap 43 (aclosing part, a cap member) is completely covered on the hoop 36. Inother words, the tip end surface of the hoop tip end portion 36 a isbrought into contact with an inner surface of the cap tip end portion 43a. Also, in Step S2, a gap may be provided between the tip end surfaceof the hoop tip end portion 36 a and the inner surface of the cap tipend portion 43 a.

Next, Step S4 is performed (refer to FIG. 5(b)). In Step S4, thecatheter 31 is accommodated in the hoop 36. Further, in Step S4, thecatheter tip end portion 31 a does not coincide with the hoop tip endportion 36 a. That is, the bellows 46 is disposed between the hoop 36and the holding plug 37. That is, the catheter 31 is accommodated in thehoop 36 so that the catheter 31 is at the first position. Specifically,the holding plug 37 is mounted on the bellows base end portion 46 b.Further, the bellows tip end portion 46 a is mounted on the base endsurface of the hoop base end portion 36 b. Here, the bellows 46 has apredetermined length in the axial direction. The predetermined lengthcorresponds to, for example, a distance from the tip end surface of thehoop tip end portion 36 a to the tip end surface of the catheter tip endportion 31 a in an accommodated state. In a procedure of performingSteps S2 and S4, Step S4 may be performed after Step S2, as describedabove. In addition, Step S2 may be performed after Step S4.

Next, Step S6 is performed (refer to FIG. 5(c)). In Step S6, thecatheter kit 30 is sterilized. Specifically, first, the catheter kit 30is put into a sterilization bag 102. Next, the sterilization bag 102 issealed. Next, the catheter kit 30 and the sterilization bag 102 areplaced inside a chamber (not shown). Next, the inside of the chamber isdegassed. Next, a sterilization gas G is supplied into the chamber. Thesterilization bag 102 formed so that one side surface is formed of vinyland the other side surface is formed of a non-woven fabric. Therefore,the sterilization gas G is filled into the bag even when thesterilization bag 102 is sealed. An example of the sterilization gas Gincludes ethylene oxide gas (EoG). Then, the catheter kit 30 issterilized by the sterilization gas G.

However, the catheter 31 is accommodated in the hoop 36. The hoop tipend portion 36 a is closed by a protection cap 43. The hoop base endportion 36 b is closed by the holding plug 37 and the bellows 46. Here,the hoop 36 has a gas introduction hole 36 e. The sterilization gas G isintroduced into the hoop 36 from the gas introduction hole 36 e.Therefore, according to the gas introduction hole 36 e, the catheter 31accommodated in the hoop 36 can be reliably sterilized. After thesterilization gas G is filled in, the sterilization gas G is degassedfrom the chamber.

The catheter kit 30 which has been sterilized by Steps S2, S4 and S6 asdescribed above is prepared.

Subsequently, a process of measuring the catheter kit 30 will bedescribed.

First, Step S8 is performed (refer to FIG. 6(a)). Specifically, thecatheter kit 30 is taken out of the sterilization bag 102. Then, thelight source 101 is connected to the optical fiber base end portion 33 bof the optical fiber 33.

Next, Step S10 is performed (refer to FIG. 6(b)). In Step S10, theholding plug 37 is pushed into the hoop 36. That is, the position of thecatheter tip end portion 31 a coincides with the position of the hooptip end portion 36 a.

Next, Step S12 is performed (refer to FIG. 7(a)). First, the catheterkit 30 is mounted in the power meter 2. More specifically, the adapter 3is screwed into the mounting part 7 of the power meter 2. Then, the tipend side (the protection cap 43 side) of the catheter kit 30 is insertedinto the adapter 3.

Next, Step S14 is performed (refer to FIG. 7(a)). Specifically, thelight source 101 is operated. As a result, the laser light L isgenerated. The laser light L is emitted from the catheter tip endportion 31 a through the optical fiber 33. The emitted laser light L isincident on the light receiving part 6. The light receiving part 6outputs an electrical signal according to the incident laser light L.The content of the signal is displayed on the processing device 8. It isconfirmed that the predetermined intensity of the laser light L isobtained on the basis of the displayed content of the signal.

Next, Step S16 is performed (refer to FIG. 7(b)). Specifically, thecatheter kit 30 is pulled out of the adapter 3. Next, the holding plug37 is pulled out of the hoop 36. As a result, the catheter 31 is takenout of the hoop 36. Then, in Step S18 (not shown), a predeterminedtreatment or examination is performed using the catheter 31.

In the light measurement device 1 according to the embodiment, themounting part 7 defines the position of the hoop 36 with respect to thelight receiving part 6. As a result, it is not necessary to take out thecatheter 31 from the hoop 36 to measure the intensity of the laser lightL. Then, it is possible to measure the intensity of the laser light L ina state in which the catheter 31 is accommodated in the hoop 36. As aresult, the cleanliness of the catheter 31 can be maintained.Furthermore, the catheter 31 does not have to be taken out of the hoop36. As a result, the process required to measure the laser light L canbe simplified. Therefore, according to the light measurement device 1,the cleanliness of the catheter 31 can be maintained, and the lightintensity confirmation operation can be easily performed.

In the catheter kit 30 according to the embodiment, the position of thecatheter 31 with respect to the hoop 36 is held by the holding plug 37.According to such a configuration, when the intensity of the laser lightL is measured, it is possible to curb occurrence of variation of adistance from the catheter tip end portion 31 a to the light receivingpart 6.

Furthermore, the catheter kit 30 further includes the positionadjustment mechanism 47 which is provided at the hoop base end portion36 b and changes the position of the catheter tip end portion 31 a withrespect to the hoop tip end portion 36 a in an extending direction ofthe hoop 36. According to such a configuration, it is possible to switchbetween the position of the catheter tip end portion 31 a at the time ofstorage and the position of the catheter tip end portion 31 a at thetime of measurement. That is, at the time of storage, the catheter tipend portion 31 a can be disposed on the inner side of the hoop tip endportion 36 a. As a result, the catheter tip end portion 31 a can beprotected. Furthermore, at the time of measurement, it is possible toalign the catheter tip end portion 31 a with the position of the hooptip end portion 36 a. As a result, it is possible to curb the occurrenceof the variation in the distance from the catheter tip end portion 31 ato the light receiving part 6.

The holding plug 37 of the catheter kit 30 holds the position of thecatheter 31 relative to the position of the hoop 36 so that the cathetertip end portion 31 a is aligned with the hoop tip end portion 36 a inthe extending direction of the hoop 36. According to such aconfiguration, the position of the hoop tip end portion 36 a is defined.As a result, the position of the catheter tip end portion 31 a isdefined. Therefore, the occurrence of the variation in the distance fromthe catheter tip end portion 31 a to the light receiving part 6 can befurther curbed.

The catheter kit 30 further includes the protection cap 43 which ismounted on the hoop tip end portion 36 a and closes the tip end opening36 c of the hoop tip end portion 36 a. According to such aconfiguration, the catheter tip end portion 31 a can be protected.

More specifically, the catheter kit 30 further includes the protectioncap 43 which is mounted on the hoop 36, and the adapter 3 which disposesthe hoop 36 on which the protection cap 43 is mounted to the mountingpart 7. The hoop 36 has the hoop tip end portion 36 a in which thecatheter tip end portion 31 a is disposed and which includes the tip endopening 36 c. The protection cap 43 is mounted on the hoop tip endportion 36 a. The protection cap 43 has the cap tip end portion 43 aincluding the transmission window 43 c which closes the tip end opening36 c and transmits the laser light L emitted from the optical fiber 33.The adapter 3 has the contact part 3 c with which the cap tip endportion 43 a is in contact. According to such a configuration, theprotection cap 43 having the transmission window 43 c is disposedbetween the catheter tip end portion 31 a and the light receiving part6. The transmission window 43 c closes the tip end opening 36 c of thehoop tip end portion 36 a. Therefore, the catheter tip end portion 31 acan be protected.

In the light measurement method according to the embodiment, theposition of the hoop 36 with respect to the light receiving part 6 isdefined in Step S12 in which the hoop 36 is disposed in the mountingpart 7. As a result, it is not necessary to take out the catheter 31from the hoop 36 to measure the intensity of the laser light L. Then, inStep S14 in which the intensity of the laser light L is obtained, it ispossible to measure the intensity of the laser light L in a state inwhich the catheter 31 is accommodated in the hoop 36. Therefore, thecleanliness of the catheter 31 can be maintained. Furthermore, thecatheter 31 does not have to be taken out of the hoop 36. As a result,the process required to measure the laser light L can be simplified.Accordingly, according to the light measurement method, the cleanlinessof the catheter 31 can be maintained, and the light intensityconfirmation operation can be easily performed.

The present invention has been described above in detail on the basis ofthe embodiments. However, the present invention is not limited to theabove-described embodiments. The present invention can be variouslymodified without departing from the scope of the invention. For example,the catheter kit is not limited to the configurations shown in theabove-described embodiments. The catheter kit can take a variety ofconfigurations.

The catheter kit 30 according to the embodiment has the configuration(the protection cap 43) which closes the tip end opening 36 c of thehoop tip end portion 36 a. The configuration which closes the tip endopening 36 c may be a configuration shown in the following first, secondand third modified examples.

Modified Example 1

As shown in FIG. 8(a), a catheter kit 30C according to a first modifiedexample has a protection cap 48. The protection cap 48 may be detachablefrom the hoop 36. Also, the protection cap 48 may be fixed to the hoop36 by an adhesive or the like so that it cannot be removed from the hoop36. The protection cap 48 is formed of a material transparent to thelaser light L. The protection cap 48 has a cap main body 48 a and aflange part 48 b. The cap main body 48 a has a cylindrical shape. Thecap main body 48 a is fitted into the hoop tip end portion 36 a. Theflange part 48 b is provided on the tip end side of the cap main body 48a. The flange part 48 b has a disk shape. The flange part 48 b has adiameter substantially the same as a diameter of the outercircumferential surface of the hoop 36. That is, the diameter of theflange part 48 b is larger than an inner diameter of the tip end opening36 c. According to such a configuration, a base end surface of theflange part 48 b is in contact with the tip end surface of the hoop tipend portion 36 a. As a result, an insertion depth of the protection cap48 can be defined.

The protection cap 48 has a catheter arrangement part 48 c which definesa position of the catheter tip end portion 31 a. The catheterarrangement part 48 c aligns a central axis A31 of the catheter 31 witha central axis A36 of the hoop 36. In other words, the catheterarrangement part 48 c defines the position of the catheter tip endportion 31 a in a radial direction of the hoop 36. Furthermore, thecatheter arrangement part 48 c also defines a direction of the catheter31 (that is, an emitting direction of the laser light L) in apredetermined direction. According to such a catheter arrangement part48 c, the position and posture of the catheter tip end portion 31 a withrespect to the light receiving part 6 can be defined with high accuracy.Therefore, it is possible to obtain an accurate light intensity value.In addition, it is possible to curb the occurrence of variations inlight intensity for each measurement.

The catheter arrangement part 48 c is a tapered hole and extends from abase end surface of the cap main body 48 a toward the flange part 48 b.A diameter of the catheter arrangement part 48 c gradually decreasestoward the flange part 48 b. The catheter arrangement part 48 c has abase end opening 48 d provided in a base end surface thereof, and abottom portion 48 e provided on the flange part 48 b side. An innerdiameter of the base end opening 48 d is larger than an outer diameterof the catheter 31. Furthermore, the inner diameter of the base endopening 48 d is slightly smaller than the inner diameter of the hoop 36.A diameter of the bottom portion 48 e is smaller than the outer diameterof the catheter 31. Therefore, the tip end surface of the catheter tipend portion 31 a is not in contact with the bottom portion 48 e.According to such a catheter arrangement part 48 c, when the catheter 31is inserted into the hoop 36 from the base end side toward the tip endside, the catheter tip end portion 31 a can be suitably guided to thecatheter arrangement part 48 c. When the protection cap 48 is used, thetip end surface of the catheter tip end portion 31 a does not protrudefrom the tip end surface of the hoop tip end portion 36 a. Therefore,the position of the catheter tip end portion 31 a in the emittingdirection of the laser light L is defined.

According to the protection cap 48, the laser light L passes through thecap main body 48 a and the flange part 48 b and is incident on the lightreceiving part 6. Specifically, a shape of the catheter arrangement part48 c may be configured so that an optical axis of the laser light Lintersects a tapered surface of the catheter arrangement part 48 c(refer to an arrow W1). The shape of the catheter arrangement part 48 cmay be configured so that the optical axis of the laser light L does notintersect the tapered surface. That is, the shape of the catheterarrangement part 48 c may be configured so that the optical axis of thelaser light L intersects the bottom portion 48 e (refer to an arrow W2).

Modified Example 2

As shown in FIG. 8(b), a catheter kit 30D according to a second modifiedexample can also regulate the position of the catheter tip end portion31 a, like the catheter kit 30C of the first modified example.

The catheter kit 30D has a protection cap 49. The protection cap 49 maybe detachable from the hoop 36. The protection cap 49 may be fixed tothe hoop 36 by an adhesive or the like so that it cannot be removed fromthe hoop 36. The protection cap 49 has a main body tubular part 49 a anda tapered tubular part 49 b. The main body tubular part 49 a is atubular member which covers the hoop tip end portion 36 a. An innerdiameter of the main body tubular part 49 a is substantially the same asor slightly smaller than the outer diameter of the hoop 36. The taperedtubular part 49 b is provided on the tip end side of the main bodytubular part 49 a. The tapered tubular part 49 b has a truncated coneshape. An outer diameter of the tapered tubular part 49 b graduallydecreases from a portion thereof which is continuous with the main bodytubular part 49 a to the tip end side. The tapered tubular part 49 b hasa tapered hole. An inner diameter of the tapered hole graduallydecreases towards the tip end. The tapered hole is a catheterarrangement part 49 c.

The catheter arrangement part 49 c is a tapered hole. The tapered holeextends from a boundary between the main body tubular part 49 a and thetapered tubular part 49 b toward the tip end. The diameter of thecatheter arrangement part 49 c gradually decreases toward the tip end.The catheter arrangement part 49 c has a base end opening 49 d and a tipend bottom portion 49 e. An inner diameter of the base end opening 49 dis substantially the same as the outer diameter of the hoop 36. Adiameter of the tip end bottom portion 49 e is smaller than the outerdiameter of the catheter 31. Therefore, the tip end surface of thecatheter tip end portion 31 a is not in contact with the tip end bottomportion 49 e. According to such a catheter arrangement part 49 c, whenthe catheter 31 is inserted into the hoop 36 from the base end side tothe tip end side, the catheter tip end portion 31 a can be suitablyguided to the catheter arrangement part 49 c. Also, when the protectioncap 49 is used, the tip end surface of the catheter tip end portion 31 aprotrudes from the tip end surface of the hoop tip end portion 36 a.According to such a configuration, the catheter tip end portion 31 a canbe brought closer to the light receiving part 6 in a state in which thecatheter tip end portion 31 a is protected.

According to the protection cap 49, the laser light L passes through thetapered tubular part 49 b and is incident on the light receiving part 6.Specifically, in a shape of the catheter arrangement part 49 c, theoptical axis of the laser light L intersects the tip end bottom portion49 e without intersecting the tapered surface (refer to an arrow W3).Also, the shape of the catheter arrangement part 49 c may be so that theoptical axis of the laser light L intersects the tapered surface.

Modified Example 3

As shown in FIG. 8(c), a catheter kit 30E according to a third modifiedexample has a protection cover part 51. The protection cover part 51 hasa disk shape. The protection cover part 51 has an outer circumferentialsurface 51 a, a tip end surface 51 b, and a base end surface 51 c. Anouter diameter of the protection cover part 51 is approximately equal tothe inner diameter of the hoop 36. The protection cover part 51 isfitted into the tip end opening 36 c of the hoop tip end portion 36 a.The tip end surface 51 b of the protection cover part 51 is exposed tothe outside. The base end surface 51 c of the protection cover part 51faces the inside of the hoop 36. That is, the catheter tip end portion31 a faces the base end surface 51 c. The laser light L emitted from thecatheter tip end portion 31 a passes through the protection cover part51 and is then incident on the light receiving part 6. Therefore, theprotection cover part 51 is formed of a material transparent to thelaser light L.

The protection cover part 51 is fixed to the hoop 36 by an adhesive orthe like so that it cannot be removable therefrom. That is, theprotection cover part 51 is integrated with the hoop 36. Specifically,the outer circumferential surface 51 a of the protection cover part 51is fixed to the inner circumferential surface of the hoop 36 by adhesionor the like. According to such a configuration, the protection coverpart 51 is not separated from the hoop 36. Therefore, the catheter tipend portion 31 a can be reliably protected.

In the catheter kit 30 according to the embodiment, the tip end opening36 c of the hoop tip end portion 36 a is open. Thus, the catheter kithaving the open end tip opening 36 c may have the configuration shown inthe following fourth, fifth, and sixth modified examples.

Modified Example 4

As shown in FIG. 9(a), a catheter kit 30F according to a fourth modifiedexample has a hoop 52. The hoop 52 has a catheter arrangement part 52 bprovided at a hoop tip end portion 52 a. The catheter arrangement part52 b aligns the central axis A31 of the catheter 31 with a central axisA52 of the hoop 52. The catheter arrangement part 52 b has a throughhole 52 c and a tapered part 52 d. The through holes 52 c are providedside by side along the central axis A52 of the hoop 52. The tapered part52 d constitutes the catheter arrangement part 52 b. The through hole 52c includes a tip end opening 52 e formed in a tip end surface of thehoop tip end portion 52 a, and a base end opening 52 f formed on thebase end side. The tapered part 52 d includes a tip end portion 52 gwhich is continuous with the base end opening 52 f, and a base endportion 52 h which is continuous with an inner circumferential surfaceof the hoop 52. An inner diameter of the through hole 52 c is smallerthan an inner diameter of the hoop 52. Accordingly, an inner diameter ofthe tapered part 52 d gradually decreases from the base end portion 52 htoward the tip end portion 52 g. Furthermore, the inner diameter of thethrough hole 52 c is smaller than the outer diameter of the catheter 31.Therefore, the catheter tip end portion 31 a is not inserted into thethrough hole 52 c.

The catheter arrangement part 52 b is a part of the hoop 52. In otherwords, the catheter arrangement part 52 b is a portion of the hoop tipend portion 52 a in which a thickness of the hoop 52 gradually increasestoward the tip end. In such a catheter arrangement part 52 b, thecatheter tip end portion 31 a does not protrude from the hoop tip endportion 52 a. Therefore, the catheter tip end portion 31 a does notprotrude from an adapter tip end surface 53 a of the adapter 53.Accordingly, the position of the catheter tip end portion 31 a in anemitting direction of the laser light L is defined.

The laser light L emitted from the catheter 31 is incident on the lightreceiving part 6 through the through hole 52 c (refer to an arrow W4).Therefore, the laser light L emitted from the catheter 31 is directlyincident on the light receiving part 6. As a result, accuratemeasurement results can be obtained. Also, the laser light L passesthrough the through hole 52 c. Therefore, the material constituting thehoop 52 may or may not be transparent to the laser light L. The hoop 52may be formed of a transparent material. In addition, the hoop 52 may beformed of a material which is not transparent to light.

Modified Example 5

As shown in FIG. 9(b), a catheter kit 30G according to a fifth modifiedexample has a hoop 54. The hoop 54 has a hoop main body 54 a and aprotruding tubular part 54 b. The hoop main body 54 a has a hoop tip endportion 54 d including a tip end surface 54 c. A central axis of theprotruding tubular part 54 b overlaps a central axis of the hoop mainbody 54 a. The protruding tubular part 54 b protrudes from the tip endsurface 54 c. An outer diameter of the protruding tubular part 54 b issmaller than an outer diameter of the hoop main body 54 a. Thus, the tipend surface 54 c of the hoop main body 54 a and an outer circumferentialsurface 54 e of the protruding tubular part 54 b form a stepped portion.

When the hoop 54 is inserted into the adapter 56, the protruding tubularpart 54 b protrudes from a tip end opening 56 b of an adapter tip endportion 56 a. The tip end surface 54 c of the hoop main body 54 a is incontact with an inner surface of the adapter tip end portion 56 a. Thetip end surface 54 c of the hoop main body 54 a defines an insertiondepth of the hoop 54 into the adapter 56.

The hoop 54 has a catheter arrangement part 54 f. The catheterarrangement part 54 f is a part of the hoop 54. The catheter arrangementpart 54 f is a tapered hole. An inner diameter of the catheterarrangement part 54 f gradually decreases from the base end side towardthe tip end side. Specifically, a base end portion 54 g of the catheterarrangement part 54 f is provided on the hoop main body 54 a. An innerdiameter of the base end portion 54 g is equal to an inner diameter ofthe hoop main body 54 a. A tip end portion 54 h of the catheterarrangement part 54 f is an opening provided in the tip end surface 54 cof the protruding tubular part 54 b. An inner diameter of the tip endportion 54 h is smaller than an inner diameter of the hoop 54.Furthermore, the inner diameter of the tip end portion 54 h is smallerthan the outer diameter of the catheter 31. The inner diameter of thecatheter arrangement part 54 f is larger than the outer diameter of thecatheter 31 at a position corresponding to the tip end surface 54 c ofthe hoop main body 54 a.

According to such a configuration, when the catheter 31 is inserted intothe catheter arrangement part 54 f the catheter tip end portion 31 a isdisposed on the tip end side from a position corresponding to the tipend surface 54 c of the hoop main body 54 a which is larger than theouter diameter of the catheter 31. Therefore, the catheter tip 31 a canbe brought closer to the light receiving part 6. As a result, anaccurate light intensity can be obtained. Further, an opening providedin the protruding tubular part 54 b is smaller than the outer diameterof the catheter 31. As a result, the catheter tip end portion 31 a doesnot protrude from the protruding tubular part 54 b to the tip end side.Therefore, the protruding tubular part 54 b protects the catheter tipend portion 31 a.

Modified Example 6

As shown in FIG. 9(c), a catheter kit 30H according to a sixth modifiedexample has a hoop 57. The hoop 57 has a hoop main body 57 a and a hoopflange part 57 b. The hoop main body 57 a has a hoop tip end surface 57c. A central axis of the hoop flange part 57 b overlaps a central axisof the hoop main body 57 a. The hoop flange part 57 b is provided at aposition spaced apart from the hoop tip end surface 57 c of the hoopmain body 57 a to the base end side by a predetermined distance. Thepredetermined distance is, for example, larger than a distance from anadapter tip end surface 58 a of an adapter 58 to an adapter base endsurface 58 b. An outer diameter of the hoop flange part 57 b is largerthan an inner diameter of the hoop arrangement part 58 d of the adapter58. Therefore, when the hoop 57 is inserted into the adapter 58, a tipend surface 57 h of the hoop flange part 57 b is in contact with theadapter 58. More specifically, the tip end surface 57 h of the hoopflange part 57 b is in contact with the adapter base end surface 58 b.The hoop flange part 57 b defines an insertion depth of the hoop 57 intothe adapter 58. A distance from a position in which the hoop flange part57 b is provided to the hoop tip end surface 57 c is larger than adistance from the adapter tip end surface 58 a to the adapter base endsurface 58 b. Therefore, when the hoop flange part 57 b is in contactwith the adapter 58, the hoop tip end surface 57 c protrudes from theadapter tip end surface 58 a.

The hoop 57 has a catheter arrangement part 57 e. The catheterarrangement part 57 e is a part of the hoop 57. The catheter arrangementpart 57 e is a tapered hole. An inner diameter of the catheterarrangement part 57 e gradually decreases from the base end side to thetip end side. Specifically, an inner diameter of the base end portion 57f of the catheter arrangement part 57 e is equal to an inner diameter ofthe hoop main body 57 a. A tip end portion 57 g of the catheterarrangement part 57 e is an opening provided in the hoop tip end surface57 c. An inner diameter of the tip end portion 57 g is smaller than aninner diameter of the hoop 57. Furthermore, the inner diameter of thetip end portion 57 g is smaller than the outer diameter of the catheter31. The inner diameter of the catheter arrangement part 57 e is largerthan the outer diameter of the catheter 31 at a position in which thehoop main body 57 a protrudes from the adapter tip end surface 58 a.

According to such a configuration, when the catheter 31 is inserted intothe catheter arrangement part 57 e, the catheter tip end portion 31 a isdisposed on the tip end side from the adapter tip end surface 58 a.Therefore, the catheter tip end portion 31 a is brought closer to thelight receiving part 6. As a result, an accurate light intensity can beobtained. Further, an opening provided in the tip end portion 57 g issmaller than the outer diameter of the catheter 31. As a result, thecatheter tip end portion 31 a does not protrude from the hoop tip endsurface 57 c to the tip end side. Therefore, the tip end portion 57 gprotects the catheter tip end portion 31 a.

The catheter kit 30 according to the embodiment has included theposition adjustment mechanism 47 which switches the position of thecatheter 31 with respect to the hoop 36. The specific configuration ofthe position adjustment mechanism may be as shown in the followingseventh and eighth modified examples.

Modified Example 7

As shown in FIG. 10 , a catheter kit 30J according to a seventh modifiedexample has a position adjustment mechanism 59 which has a differentstructure from that in the embodiment. The position adjustment mechanism59 is a tube 59 a formed of silicone rubber or the like. The tube 59 ais disposed between the hoop 36 and the holding plug 61. The tube 59 amaintains and changes a gap between the hoop base end portion 36 b and aholding plug tip end surface 61 a.

The hoop base end portion 36 b is inserted into a tube tip end portion59 b. A press-fit part 61 b of the holding plug 61 is inserted into atube base end portion 59 c. In other words, the position adjustmentmechanism 59 is a double structure configured with the tube 59 a and thehoop 36. Here, the tube base end portion 59 c is fixed to the holdingplug 61. On the other hand, the tube tip end portion 59 b is slidablewith respect to the hoop base end portion 36 b. Such a configuration canbe realized by setting an inner diameter of the tube tip end portion 59b and an outer diameter of the hoop base end portion 36 b topredetermined dimensional values.

As shown in FIG. 10(a), when the catheter kit 30J is stored or the like,the tube 59 a maintains a gap between the hoop base end portion 36 b andthe holding plug tip end surface 61 a at a predetermined distance. Atthis time, the catheter tip end portion 31 a is disposed on the base endside by a gap with respect to the hoop tip end portion 36 a (the firstposition). That is, the catheter tip end portion 31 a is protected bythe hoop 36.

As shown in FIG. 10(b), when the measurement of the laser light L isperformed using the catheter kit 30J, the holding plug 61 is pushed tothe tip end side. Then, slippage occurs between the tube tip end portion59 b and the hoop base end portion 36 b. As a result, the tube 59 a andthe holding plug 61 move integrally to the tip end side. That is, thegap between the hoop base end portion 36 b and the holding plug tip endsurface 61 a is reduced. Then, finally, the holding plug tip end surface61 a comes into contact with the hoop base end portion 36 b. At thistime, the catheter tip end portion 31 a coincides with the position ofthe hoop tip end portion 36 a. That is, the catheter tip end portion 31a is disposed at a position (the second position) suitable formeasurement of the light intensity.

Modified Example 8

As shown in FIG. 11 , a catheter kit 30K according to an eighth modifiedexample may have a position adjustment mechanism 62 having anotherconfiguration. The position adjustment mechanism 62 is configured with aguide pin 62 a and a guide groove 62 b. The guide pin 62 a and the guidegroove 62 b reliably switch between a state in which the catheter tipend portion 31 a is protected and a state in which the measurement ofthe laser light L is performed using the catheter kit 30K. Furthermore,the position adjustment mechanism 62 can reliably maintain each of thestates. The catheter kit 30K has a tube 63. The tube 63 is disposedbetween the hoop 64 and the holding plug 65. That is, like the positionadjustment mechanism 62 according to the seventh modified example, theposition adjustment mechanism 62 according to the eighth modifiedexample has a so-called double structure.

For example, the guide groove 62 b is provided in the outercircumferential surface of the hoop base end portion 64 a. The guidegroove 62 b may penetrate the side wall of the hoop 64. Also, the guidegroove 62 b may have a bottom portion. The guide groove 62 b includes afirst restricting part 62 c and a second restricting part 62 d whichextend in a circumferential direction, and a connecting groove part 62 ewhich extends in an axial direction. One end of the first restrictingpart 62 c and one end of the second restricting part 62 d are connectedby the connecting groove part 62 e. The connecting groove part 62 eextends in the axial direction of the hoop 64. The first restrictingpart 62 c is provided on the hoop base end surface side. The secondrestricting part 62 d is provided on the tip end side from the firstrestricting part 62 c. A distance from the first restricting part 62 cto the second restricting part 62 d corresponds to a movement distanceof the catheter 31. The guide pin 62 a is provided on an innercircumferential surface of the tube 63. The guide pin 62 a is acylindrical protrusion. The guide pin 62 a extends from the innercircumferential surface of the tube 63 in the radial direction thereof.A diameter of the guide pin 62 a is substantially the same as orslightly smaller than that of the guide groove 62 b.

As shown in FIG. 11(a), when the catheter kit 30K is stored or the like,the guide pin 62 a is fitted into the first restricting part 62 c. Whenthe guide pin 62 a is fitted into the first restricting part 62 c, thecatheter tip end portion 31 a is in a protected state in which it isdisposed on the inner side of the hoop 64 (at the first position). Thefirst restricting part 62 c extends in the circumferential direction. Asa result, the guide pin 62 a does not move in the axial direction.Therefore, since the catheter tip end portion 31 a is disposed at theinner side of the hoop 64, the protected state can be reliablymaintained.

Next, a switching operation will be described. As shown in FIG. 11(b),first, the tube 63 is rotated in a direction in which the firstrestricting part 62 c extends. Then, the guide pin 62 a moves to thebase end of the connecting groove part 62 e. Then, the guide pin 62 a ismoved along the connecting groove part 62 e. That is, the tube 63 andthe holding plug 65 are moved to the tip end side. Due to this movement,the catheter tip end portion 31 a coincides with the hoop tip endportion 36 a. Then, after the guide pin 62 a is moved to the tip end ofthe connecting groove part 62 e, the tube 63 is rotated in thecircumferential direction. Then, the guide pin 62 a is fitted into thesecond restricting part 62 d. When the guide pin 62 a is fitted into thesecond restricting part 62 d, the catheter tip end portion 31 a is in ameasurement state in which it coincides with the hoop tip end portion 36a (the second position). The second restricting part 62 d extends in thecircumferential direction, like the first restricting part 62 c. As aresult, the guide pin 62 a does not move in the axial direction.Therefore, a state in which the catheter tip end portion 31 a isdisposed at the hoop tip end portion 36 a can be reliably maintained.

The catheter kit 30 according to the embodiment has the mechanism forholding the position of the catheter 31 with respect to the hoop 36. Thespecific configuration of the mechanism may be as shown in the followingninth, tenth and eleventh modified examples.

Modified Example 9

As shown in FIG. 12(a), a catheter kit 30L according to a ninth modifiedexample may have a clip 66 as the mechanism for holding the position ofthe catheter 31. The clip 66 is mounted on the hoop base end portion 36b. The clip 66 generates a force as if it crushes the hoop 36 in theradial direction. When the hoop 36 is crushed in the radial direction,the inner circumferential surface of the hoop 36 is in tight contactwith the outer circumferential surface of the catheter 31. The clip 66is mounted to sandwich the hoop 36 in the radial direction. Therefore,side walls of the hoop 36 crushed by the clip 66 sandwich the catheter31. According to such a configuration, the position of the catheter 31with respect to the hoop 36 is maintained. Also, when the hoop 36 ismoved, the clip 66 is removed. According to the holding mechanism by theclip 66, it is possible to easily switch between a state in which thecatheter 31 is held and a state in which the catheter can be moved.

Modified Example 10

As shown in FIG. 12(b), a catheter kit 30P according to a tenth modifiedexample may have a tube 67 as the holding mechanism. The configurationis similar to the configuration of the seventh modified example. Thatis, it has a double structure. The difference from the configuration ofthe seventh modified example is that it is difficult for the tube tipend portion 67 a to slide with respect to the hoop base end portion 36b. In the tenth modified example, the inner diameter of the tube 67 issmaller than the outer diameter of the hoop 36. As a result, when thehoop 36 is inserted into the tube 67, a press-fit state is obtained.

Modified Example 11

As shown in FIG. 12(c), a catheter kit 30Q according to an eleventhmodified example may have a clamp 68 as the holding mechanism. The clamp68 is a U-shaped component capable of detachably mounting the catheterbase end portion 31 b. The clamp 68 includes a fixing part 69 which isfixed to the outer circumferential surface of the hoop 36. The catheterbase end portion 31 b is inserted from an opening of the clamp 68 in theradial direction. As a result, the catheter base end portion 31 b isfixed to the clamp 68. The clamp 68 is then fixed to the hoop 36 by thefixing part 69. Thus, the catheter 31 is held with respect to the hoop36.

The catheter kit 30 according to the embodiment has the protection cap43 which is mounted on the hoop tip end portion 36 a at the time ofstorage. The configuration for protecting the catheter tip end portion31 a disposed to coincide with the hoop tip end portion 36 a may beconfigured as shown in the following twelfth and thirteenth modifiedexamples.

Modified Example 12

As shown in FIGS. 13(a) and 13(b), a catheter kit 30S according to atwelfth modified example has a protection cap 72. The protection cap 72has a configuration similar to that of the protection cap 72 of thesecond modified example. The difference from the protection cap 49 ofthe second modified example is that the protection cap 72 according tothe twelfth modified example can be moved with respect to the hoop 36.

As shown in FIG. 13(a), when the catheter kit 30S is stored, theprotection cap 72 is shallowly covered on the hoop tip end portion 36 a.According to such a configuration, a space is provided between the captip end portion 72 a of the protection cap 72 and the catheter tip endportion 31 a. Therefore, the catheter tip end portion 31 a can beappropriately protected.

On the other hand, as shown in FIG. 13(b), when the measurement of thelaser light L using the catheter kit 30S is performed, the protectioncap 72 is pushed to the hoop 36 side. A distance between a cap tip endportion 72 a and the catheter tip end portion 31 a is reduced by thepushing. Then, when the protection cap 72 and the hoop 36 are regardedas one hoop member, the protection cap 72 changes a relative positionbetween the catheter tip end portion 31 a and the hoop member.Accordingly, the protection cap 72 may be defined as a broad positionadjustment mechanism. Furthermore, the catheter tip end portion 31 a isguided along a tapered inner circumferential surface of the protectioncap 72. As a result of this guidance, the central axis A31 of thecatheter 31 follows the central axis A36 of the hoop 36. Therefore, thevariations in the position and posture of the catheter tip end portion31 a from which the laser light L is emitted are curbed. As a result,accurate measurement of light intensity can be performed.

Modified Example 13

As shown in FIG. 13(c), a catheter kit 30R according to a thirteenthmodified example has a protection tube 71. The protection tube 71 ismounted to the hoop tip end portion 36 a. As a result, the hoop 36substantially extends. The protection tube 71 has a tube base endportion 71 a which receives the hoop tip end portion 36 a, and a tubetip end portion 71 b. When the tube base end portion 71 a is mounted tothe hoop tip end portion 36 a, the substantial tip end of the hoop 36 isthe tube tip end portion 71 b. The tube tip end portion 71 b protrudesfurther to the tip end side than the hoop tip end portion 36 a.Therefore, the catheter tip end portion 31 a is disposed on the base endside from the tube tip end portion 71 b. According to such aconfiguration, the protection tube 71 protects the catheter tip endportion 31 a. Additionally, when the measurement of the laser light L isperformed, the protection tube 71 is removed.

The catheter kit may be freely combined with the first to sixth, twelfthand thirteenth modified examples of the tip end shape, the seventh andeighth modified examples of the position adjustment mechanism, and theninth, tenth and eleventh modified examples of the holding mechanismaccording to conditions required for the catheter kit.

REFERENCE SIGNS LIST

-   -   1 Light measurement device    -   2 Power meter    -   3 Adapter    -   3 b Adapter base end surface    -   3H Hoop arrangement part    -   3Hb Base end opening    -   4 Case body    -   6 Light receiving part    -   7 Mounting part    -   7 a Standing tubular part    -   7 b Mounting end surface    -   7H Adapter arrangement part    -   7Ha Tip end opening    -   7Hb Base end opening    -   8 Processing device    -   9 Adapter main body    -   11 Adapter flange    -   30, 30C, 30D, 30E, 30F, 30G, 30H, 30J, 30K, 30L, 30P, 30Q, 30R,        30S Catheter kit    -   31 Catheter    -   31 a Catheter tip end portion    -   31 b Catheter base end portion    -   32 Catheter accommodating tool    -   33 Optical fiber    -   33 a Optical fiber tip end portion    -   33 b Optical fiber base end portion    -   34 Component    -   36 Hoop    -   36 a Hoop tip end portion    -   36 b Hoop base end portion    -   36 c Tip end opening    -   36 d Base end opening    -   36 e Gas introduction hole    -   37 Holding plug    -   38 Catheter arrangement part    -   39 Press-fit part    -   41 Flange part    -   43 Protection cap    -   43 a Cap tip end portion    -   43 b Cap base end portion    -   43 c Transmission window    -   43H Hoop arrangement part    -   43Hb Base end opening    -   46 Bellows    -   46 a Bellows tip end portion    -   46 b Bellows base end portion    -   47 Position adjustment mechanism    -   48 Protection cap    -   48 a Cap main body    -   48 b Flange part    -   48 c Catheter arrangement part    -   48 d Base end opening    -   48 e Bottom portion    -   49 Protection cap    -   49 a Main body tubular part    -   49 b Tapered tubular part    -   49 c Catheter arrangement part    -   49 d Base end opening    -   49 e Tip end bottom portion    -   51 Protection cover part    -   51 a Outer circumferential surface    -   51 b Tip end surface    -   51 c Base end surface    -   52 Hoop    -   52 a Hoop tip end portion    -   52 b Catheter arrangement part    -   52 c Through hole    -   52 d Tapered part    -   52 e Tip end opening    -   52 f Base end opening    -   52 g Tip end portion    -   52 h Base end portion    -   53 Adapter    -   54 Hoop    -   54 a Hoop main body    -   54 b Protruding tubular part    -   54 c Tip end surface    -   54 d Hoop tip end portion    -   54 e Outer circumferential surface    -   54 f Catheter arrangement part    -   54 g Base end portion    -   54 h Tip end portion    -   56 Adapter    -   56 a Adapter tip end portion    -   56 b Tip end opening    -   57 Hoop    -   57 a Hoop main body    -   57 b Hoop flange part    -   57 c Hoop tip end surface    -   57 e Catheter arrangement part    -   57 f Base end portion    -   57 g Tip end portion    -   57 h Tip end surface    -   58 Adapter    -   58 a Adapter tip end surface    -   58 b Adapter base end surface    -   58 d Hoop arrangement part    -   59 Position adjustment mechanism    -   59 a Tube    -   59 b Tube tip end portion    -   59 c Tube base end portion    -   61 Holding plug    -   61 a Holding plug tip end surface    -   61 b Press-fit part    -   62 Position adjustment mechanism    -   62 a Guide pin    -   62 b Guide groove    -   62 c First restricting part    -   62 d Second restricting part    -   62 e Connecting groove part    -   63 Tube    -   64 Hoop    -   64 a Hoop base end portion    -   65 Holding plug    -   66 Clip    -   67 Tube    -   67 a Tube tip end portion    -   68 Clamp    -   69 Fixing part    -   71 Protection tube    -   71 a Tube base end portion    -   71 b Tube tip end portion    -   72 Protection cap    -   72 a Cap tip end portion    -   102 Sterilization bag    -   101 Light source    -   L Laser light    -   G Sterilization gas

The invention claimed is:
 1. A catheter kit comprising: a catheterhaving an optical fiber; and a catheter accommodating tool whichaccommodates the catheter, wherein the catheter accommodating toolincludes a tubular hoop, and a position adjustment mechanism provided atthe hoop, the hoop has a hoop tip end portion at which a catheter tipend portion from which light transmitted through the optical fiber isemitted, is disposed, and a hoop base end portion which is opposite tothe hoop tip end portion, the position adjustment mechanism changes aposition of the catheter tip end portion with respect to the hoop tipend portion, the position adjustment mechanism switches between a firstposition in which the catheter tip end portion is disposed closer to thehoop base end portion relative to the hoop tip end portion, and a secondposition in which a position of the catheter tip end portion coincideswith a position of the hoop tip end portion, and the catheteraccommodating tool is disposed between an end surface of the hoop baseend portion and the position adjustment mechanism, and the positionadjustment mechanism comprises a bellows capable of extending andcontracting in an axial direction of the hoop.
 2. The catheter kitaccording to claim 1, wherein: the catheter accommodating tool furtherincludes a closing part provided at the hoop tip end portion, and theclosing part has a transmission window which transmits the light emittedfrom the catheter.
 3. The catheter kit according to claim 2, wherein:the end portion of the hoop has an opening, the catheter tip endportion, from which the light transmitted through the optical fiber isemitted, is disposed at the end portion of the hoop, and thetransmission window closes the opening and transmits the light.
 4. Thecatheter kit according to claim 3, wherein the closing part is a capmember which is detachably mounted on the hoop.
 5. The catheter kitaccording to claim 2, wherein the closing part is a cover part which isa part of the hoop and is integrated with the hoop.
 6. The catheter kitaccording to claim 1, wherein the hoop has a through hole which extendsin a direction intersecting a longitudinal direction of the hoop andextends from an outer circumferential surface to an innercircumferential surface.